Risultati della ricerca - Matthis Synofzik
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Affective coding: the emotional dimension of agency di Antje Gentsch, Matthis Synofzik
Pubblicazione 2014Artigo -
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Overcoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathways di Matthis Synofzik, Rebecca Schüle
Pubblicazione 2017Revisão -
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The Cerebellum Updates Predictions about the Visual Consequences of One's Behavior di Matthis Synofzik, Axel Lindner, Peter Thier
Pubblicazione 2008Artigo -
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The experience of agency: an interplay between prediction and postdiction di Matthis Synofzik, Gottfried Vosgerau, Martin Voss
Pubblicazione 2013Artigo -
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I move, therefore I am: A new theoretical framework to investigate agency and ownership di Matthis Synofzik, Gottfried Vosgerau, Albert Newen
Pubblicazione 2008Artigo -
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The Cerebellum Optimizes Perceptual Predictions about External Sensory Events di Manuel Jan Roth, Matthis Synofzik, Axel Lindner
Pubblicazione 2013Artigo -
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Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular Therapies di Matthis Synofzik, Hélène Puccio, Fanny Mochel, Lüdger Schöls
Pubblicazione 2019Revisão -
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Fampridine and Acetazolamide in EA2 and Related Familial EA di Carolin Muth, Julian Teufel, Lüdger Schöls, Matthis Synofzik, Christiana Franke, Dagmar Timmann, Ulrich Mansmann, Michael Strupp
Pubblicazione 2020Artigo -
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As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort di Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik
Pubblicazione 2023Carta -
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Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort di Stefanie Krüger, Florian Battke, Andrea Sprecher, Marita Munz, Matthis Synofzik, Lüdger Schöls, Thomas Gasser, Torsten Grehl, Johannes Prudlo, Saskia Biskup
Pubblicazione 2016Artigo -
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Preparing n-of-1 Antisense Oligonucleotide Treatments for Rare Neurological Diseases in Europe: Genetic, Regulatory, and Ethical Perspectives di Matthis Synofzik, Willeke M. C. van Roon‐Mom, Georg Marckmann, Hermine A. van Duyvenvoorde, Holm Graeßner, Rebecca Schüle, Annemieke Aartsma‐Rus
Pubblicazione 2021Artigo -
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Strumenti per la ricerca:
Soggetti correlati
Medicine
Biology
Genetics
Neuroscience
Disease
Pathology
Psychology
Internal medicine
Ataxia
Gene
Psychiatry
Dementia
Frontotemporal dementia
Spinocerebellar ataxia
Cerebellar ataxia
Phenotype
Mutation
Cohort
Physical medicine and rehabilitation
Allele
C9orf72
Atrophy
Trinucleotide repeat expansion
Biomarker
Neurodegeneration
Pediatrics
Oncology
Cognition
Frontotemporal lobar degeneration
Missense mutation